Abstract
The first total synthesis of (±)-senoxepin3 is described.3 is prepared via an intramolecular [4+2] cycloaddition from a substituted decadienyne7. The resulting hexalin8 was converted to a lactone, which on epoxidation, NBS bromination and elimination with NaI afforded senoxepin.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callSimilar Papers
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
